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    <title>Accessible Tables Consent Form</title>
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  <body>
    <span class="email encrypted">6577</span>
    <h1>Carnegie Mellon University &mdash; Consent Form for Participation in Research</h1>
    <h2 class="offscreen">Study Title: <span id="title">Utility of tabular structure for nonvisual browsing</span></h2>
    <main>
    <dl>
      <dt>Purpose of this Study</dt>

      <dd>
        <p>
	  The purpose of the study is to determine whether websites
	  presenting data as tables are easier to use with a screen
	  reader than websites presenting the same information as a
	  formatted list.
        </p>
      </dd>
      
      <dt>Procedures</dt>

      <dd>
	<p>
	  You will be asked to complete a series of lookup tasks on
	  websites which may be presented in various formats.  Each
	  task will be presented as a web form.  Each form will pose a
	  question whose answer is contained within a single linked
	  website.  You should answer the question as accurately as
	  possible, working at a speed comfortable to you.
	</p>

	<p>
	  Additionally, you will be asked to complete a brief online
	  survey relating to your expertise using a screen reader.
	</p>

	<p>
	  After completion of the tasks, you may be asked a series of
	  follow-up questions about problems you might have
	  encountered during the tasks.  At this time, you are also
	  welcome to point out problems with the tasks or things that
	  you noticed.
	</p>

	<p>
	  Your interactions with the task web forms will be logged for
	  subsequent analysis.  Your voice and any actions appearing
	  on the screen will also be recorded, as will the audio of
	  the follow-up interview.
	</p>

	<p>
	  The duration of the study will be 60-90 minutes.  The study
	  will take place in a designated lab on Carnegie Mellon
	  campus, or in your customized workspace.
	</p>
      </dd>

      <dt>Participant Requirements</dt>

      <dd>
	To participate in the study you must be older than 18.
	Additionally, study participants should be experienced users
	of screen readers.
      </dd>

      <dt>Risks</dt>

      <dd>
	The risks and discomfort associated with participation in this
	study are no greater than those ordinarily encountered in
	daily life, during ordinary internet use, or during routine
	psychological examinations or tests.  There is a small risk
	that other people will find out that you participated in this
	study, though we will make every effort to avoid such a breach
	of your confidentiality.
      </dd>
      
      <dt>Benefits</dt>

      <dd>
	There may be no personal benefit from your participation in
	the study but the knowledge received may be of value to
	humanity.
      </dd>
	
      <dt>Compensation &amp; Costs</dt>

      <dd>
	<p>
	  You will be paid $25 per hour for participating in this
	  study.  If you finish or the study in less than 60 minutes,
	  you will be paid for the full hour.  If you decide to
	  terminate the study at any time, you will be paid for the
	  time you spent participating.
	</p>
	<p>
	  There will be no cost to you if you participate in this study.
	</p>
      </dd>
      
      <dt>Confidentiality</dt>

      <dd>
	<p>
	  By participating in the study, you understand and agree that
	  Carnegie Mellon may be required to disclose your consent
	  form, data and other personally identifiable information as
	  required by law, regulation, subpoena or court
	  order. Otherwise, your confidentiality will be maintained in
	  the following manner:
	</p>
	<p>
	  To protect your identity, you will be assigned and told a
	  unique number.  All collected data will refer to this
	  number, not to your name.  Any publication or dissemination
	  of the research data and/or results will not contain your
	  name or any personal identifiers.  All collected recordings
	  and data files will be stored in a secured location accessed
	  only by authorized researchers, and personal identifiers
	  (including your name) will not be disclosed except by legal
	  requirement as described above.
	</p>
	<p>
	  Your data and consent form will be kept separate. Your
	  consent form will be stored in a locked location on Carnegie
	  Mellon property and will not be disclosed to third
	  parties. By participating, you understand and agree that the
	  data and information gathered during this study may be used
	  by Carnegie Mellon and published and/or disclosed by
	  Carnegie Mellon to others outside of Carnegie
	  Mellon. However, your name, address, contact information and
	  other direct personal identifiers in your consent form will
	  not be mentioned in any such publication or dissemination of
	  the research data and/or results by Carnegie Mellon.
	</p>
      </dd>
      
      <dt>Optional Permission</dt>

      <dd>
	I understand that the researchers may want to use a short
	portion of any video or audio recording for illustrative
	reasons in presentations of this work for scientific or
	educational purposes. 
        <div class="sigline1">
          <div>
            <span class="zoom">
              <input type="radio" name="video" class="videoradio"
	      value="yes" id="optin"></input>
            </span>
            <label for="optin">I give my permission to do so provided that
	      my name and face will not appear.</label>
	    <span class="initial">INITIAL HERE:</span>
	    <input type="text"/>
          </div>
          <div>
            <span class="zoom">
              <input type="radio" name="video" class="videoradio"
              value="no" id="optout"></input>
            </span>
            <label for="optout">I do not give my permission.</label>
          </div>
          <div style="display: none">
            <input type="radio" name="video" class="videoradio"  value="default" checked="true">I have not made a selection</input>
          </div>
        </div>
      </dd>
     
      <dt>Rights</dt>

      <dd>
	<p>
	  Your participation is voluntary. You are free to stop your
	  participation at any point. Refusal to participate or
	  withdrawal of your consent or discontinued participation in
	  the study will not result in any penalty or loss of benefits
	  or rights to which you might otherwise be entitled. The
	  Principal Investigator may at his/her discretion remove you
	  from the study for any of a number of reasons. In such an
	  event, you will not suffer any penalty or loss of benefits
	  or rights which you might otherwise be entitled.
	</p>
	<p>
	  At your discretion, you may arrange for assistance from any
	  people, devices or animals in completing any or all parts of
	  the study.
	</p>
      </dd>
      
      <dt>Right to Ask Questions &amp; Contact Information</dt>

      <dd>
	<p>
	  An electronic version of this document was provided to you
	  before the study, and is available at <a class="vizlink"
	  href="www.google.com">GHI</a>.  A QR code is provided at the
	  bottom right of the last page, and at the top right of the
	  first page, of this document.
	</p>
	<p>
	  If you have any questions about this study, you should feel
	  free to ask them at any time before or during the study. If
	  you have questions later, desire additional information, or
	  wish to withdraw your participation please contact the
	  Principal Investigator by mail, phone or e-mail in
	  accordance with the contact information listed in this
	  document.
	</p>
	<p>
	  If you have questions pertaining to your rights as a
	  research participant; or to report concerns to this study,
	  you should contact the Office of Research Integrity and
	  Compliance at Carnegie Mellon University. Email:
	  irb-review@andrew.cmu.edu . Phone: 412-268-1901 or
	  412-268-5460.
	</p>
	<span class="email encrypted">6540616e6472</span>	    
      </dd>

      <!--
	  Conflict of Interest

	  [In this section, please disclose any conflict of interests
	  the researchers may have with this research study, including
	  but not limited to, financial conflicts of interests. If
	  there are no conflicts of interest, please delete this
	  section]
	-->

      <dt style="page-break-before: always">Voluntary Consent</dt>

      <dd>
	<p>
	  By signing below, you agree that you have read and
	  understood the above information and that all your current
	  questions have been answered. You are encouraged to ask
	  questions about any aspect of this research study during the
	  course of the study and in the future. By signing this form,
	  you agree to participate in this research study.
	</p>
        <div class="sigline">
          <div>
	    <span class="signature participant">PARTICIPANT SIGNATURE</span>
            <span class="spacer" _aria-hidden="true">&nbsp;</span>
            <span class="date">DATE</span>
          </div>
        </div>

	<p>
	  I certify that I have explained the nature and purpose of
	  this research study to the above individual and I have
	  discussed the potential benefits and possible risks of
	  participation in the study.  The above individual has been
	  provided an electronic copy of this form, as well as a
	  signed paper copy.  Any questions the individual has about
	  this study have been answered and any future questions will
	  be answered as they arise.
	</p>
	
        <div class="sigline">
          <div>
	    <span class="signature participant">SIGNATURE OF PERSON OBTAINING CONSENT</span>
            <span class="spacer" _aria-hidden="true">&nbsp;</span>
            <span class="date">DATE</span>
         </div>
        </div>
      </dd>
    </dl>
    </main>
    <div class="email encrypted">e636d752e7367617264696e</div>  
    <header class="insitu">
      <hr/>
      <div class="qr">
	A copy of this form is<br/>
	available at <br/>
	<a href="www.google.com" class="vizlink">DEF</a>
	<br/>
	<br/>
	<a href="www.google.com" class="qrlink">ABC</a>
      </div>
      <dl>
	<dt>Study Title</dt>
	<dd class="title copy">Utility of tabular structure for nonvisual browsing</dd>
	
	<dt>Principal Investigator</dt>
	<dd>
	  <div>Steven Gardiner, PhD student</div>
          <div class="email decrypted">junkmail@yahoo.com</div>  
	  <div>Language Technologies Institute, Carnegie Mellon, GHC 6405</div>
	</dd>
	
	<dt>Faculty Advisor</dt>
	<dd>Anthony Tomasic, Systems Scientist, ISR</dd>
	
	<dt>Other Investigator</dt>
	<dd>John Zimmerman, Associate Professor, HCI</dd>

        <!--
	<dt>Sponsor</dt>
	<dd> [Insert the name of the sponsor(s)]</dd>
        -->
      </dl>
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    <div class="email encrypted">6564752</div>	    
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	A copy of this form is<br/>
	available at <br/>
	<a href="www.google.com" class="vizlink">DEF</a>
	<br/><br/>
	<a href="www.google.com" class="qrlink">ABC</a>
      </div>      
      <dl>
	<dt>IRB No</dt>
	<dd>HS15-141</dd>

	<dt>Approved</dt>
	<dd>03/24/2015</dd>

	<dt>Expires</dt>
	<dd>03/23/2016</dd>

	<dt>Modified</dt>
	<dd></dd>
      </dl>
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